Canonical Allele Identifier: CA360377199

Gene: ADGRV1

Linked Data

• dbSNP Id: rs2150014838
• MyVariant Identifiers: chr5:g.90059141T>C (hg19) ; chr5:g.90763324T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763324T>C , CM000667.2:g.90763324T>C	GRCh38
NC_000005.9:g.90059141T>C , CM000667.1:g.90059141T>C	GRCh37
NC_000005.8:g.90094897T>C	NCBI36
NG_007083.1:g.209525T>C
NG_007083.2:g.238981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12140T>C MANE Select	ENSP00000384582.2:p.Leu4047Pro
ENST00000425867.3:c.1094T>C	ENSP00000392618.3:p.Leu365Pro
ENST00000639431.1:c.265+87115T>C	ENSP00000491057.1:n.265+87115T>C
ENST00000640464.1:n.2559T>C
ENST00000640729.1:n.717T>C
ENST00000405460.6:c.12140T>C	ENSP00000384582.2:p.Leu4047Pro
NM_032119.3:c.12140T>C	NP_115495.3:p.Leu4047Pro
NR_003149.1:n.12153T>C
XM_011543675.1:c.12137T>C	XP_011541977.1:p.Leu4046Pro
XM_011543676.1:c.12059T>C	XP_011541978.1:p.Leu4020Pro
XM_011543677.1:c.9443T>C	XP_011541979.1:p.Leu3148Pro
XM_011543678.1:c.12140T>C	XP_011541980.1:p.Leu4047Pro
NM_032119.4:c.12140T>C MANE Select	NP_115495.3:p.Leu4047Pro
XM_017009963.2:c.12161T>C	XP_016865452.1:p.Leu4054Pro
XM_017009964.2:c.12158T>C	XP_016865453.1:p.Leu4053Pro
XM_017009965.1:c.12158T>C	XP_016865454.1:p.Leu4053Pro
XM_017009966.2:c.12080T>C	XP_016865455.1:p.Leu4027Pro
XM_017009967.1:c.12065T>C	XP_016865456.1:p.Leu4022Pro
XM_017009968.2:c.12161T>C	XP_016865457.1:p.Leu4054Pro
XM_017009969.2:c.12161T>C	XP_016865458.1:p.Leu4054Pro
XM_017009970.2:c.12161T>C	XP_016865459.1:p.Leu4054Pro
XM_017009971.2:c.12161T>C	XP_016865460.1:p.Leu4054Pro
XM_017009972.1:c.5279T>C	XP_016865461.1:p.Leu1760Pro
XM_017009973.1:c.5258T>C	XP_016865462.1:p.Leu1753Pro
NR_003149.2:n.12156T>C